FDA Medical Device Recalls (openFDA)
Southwest Technologies Inc: Stimulen Collagen Moisturizing Lotion, ST9555B
- Recall number
- Z-2109-2021
- Recalling firm
- Southwest Technologies Inc
- Product
- Stimulen Collagen Moisturizing Lotion, ST9555B
- Status
- Open, Classified
- Initiated
- 2021-05-28
- Posted
- not on file
- Terminated
- not on file
- Reason
- Dose audit failure after sterilization process
- Root cause
- Under Investigation by firm
- Action
- The firm notified its sold consignee of the issue by telephone on 05/28/2021 of the issue. The firm followed with a letter disseminated by letter on 06/18/2021 requesting that the distributor destroy any product on hand and notify their customers.
- Quantity
- 2016 units
- Distribution
- Malaysia
- Lot, serial or model codes
- Lot 2104007, EXP: 02/2024
- 510(k) numbers
- ["K030774"]
- PMA numbers
- not on file
- Product code
- KGN
- Firm FEI
- 1929833
- Firm city
- Kansas City
- Firm state
- MO
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28